Jump to Section 1. Introduction 2. Objectives/aims 3. Study design 3.1. Overview 3.2. Recruitment 3.3. Inclusion/exclusion criteria 3.4. Ethics 4. Procedures 4.1. Overview 4.2. Enrollment 4.3. Clinical arm 4.4. Clinical ratings and diagnoses 4.4.1. Overview 4.4.2. CDR plus NACC FTLD 4.4.3. A/L FTLD-CDR classification 4.4.4. Clinicogenetic classification 4.4.5. A/L clinical diagnosis and confidence rating form 4.4.5.1. MCI behavior 4.4.5.2. Accessing data 4.5. Biofluid arm—blood 4.5.1. A/L blood biofluid sample processing 4.5.2. Accessing data/samples 4.6. Biofluid arm—CSF 4.6.1. A/L CSF biofluid sample processing 4.6.2. Accessing data/samples 4.7. MRI arm 4.7.1. Acquisition 4.7.2. Processing 4.8. Clinical genetics arm 4.9. Research genetic and proteomic…
Read more…